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临床试验/NCT06622239
NCT06622239尚未招募2 期

A Randomized, Double-Blinded Clinical Trial to Evaluate the Effects of Naltrexone in Improving Nonsuicidal Self-injurious Behavior

Seoul National University Hospital2 个研究点 分布在 2 个国家目标入组 150 人开始时间: 2026年6月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
尚未招募
入组人数
150
试验地点
2
主要终点
Frequency of nonsuicidal self-injurous behavior

研究概览

简要总结

The goal of this clinical trial is to learn if naltrexone works to treat nonsuicidal self-injurious behavior in adolescents and adults.

详细描述

Recruiting participants with nonsuicidal self-injurious behavior and randomizing them to the experiment group and the control group at a 1:1 ratio, the test group administers the experiment drug naltrexone along with the general treatment, and the control group provides a placebo. Clinical evaluation including the frequency of self-injurious behavior is conducted every two weeks. The investigator and participants will double-blinded. Analyze the relationship between changes in clinical symptoms and socio-demographic characteristics, diagnosis, clinical characteristics, and anticipated to discover predictors of treatment effectiveness.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
16 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age: 16 years of age or older
  • Clinical interviews meet DSM-5's nonsuicidal self-injury diagnostic criteria
  • Nonsuicidal self-injurious behavior has been observed more than once in the past two months
  • Obsessive Compulsive Drinking Scale general craving item 2 or more points (strong desire)
  • Self-injurious behavior continues even with 4 weeks of general psychiatric treatment for underlying disease
  • Anyone who can independently read and fill out the questionnaire and speak Korean
  • Who understand the written consent and voluntarily agree to participate in the study
  • Female participants of childbearing age must be negative on urine pregnancy test at screening

排除标准

  • currently in psychotic or manic conditions
  • currently experiencing serious suicidal thoughts
  • history of substance-related disorders including opioid
  • do not agree to use very effective contraception from the time of signing the test subject's consent form to the end of study period (non-fertility women and postmenopausal women excluded from the contraception requirements)
  • Severe medical conditions (angina pectoris, myocardial infarction, arrhythmia, any cancer that is not in remission, hypothyroidism, hyperthyroidism, diabetes, hepatitis B, hepatitis C, epilepsy, dementia, HIV infection)
  • intellectual disability or organic brain damage
  • difficulty reading and writing Korean
  • taking opioid antagonists (methadone, buprenorphine, etc.)
  • on an opiate painkiller
  • currently opiate dependence
  • acute opiate withdrawal symptoms
  • naloxone-induced test is positive or the urine test is positive for opiates
  • have been sensitized to this drug
  • acute hepatitis, liver failure, severe liver failure
  • renal disease
  • hypersensitivity reaction to the main ingredient or other ingredients of this drug
  • a pregnant woman, a woman who may be pregnant, or a lactating woman
  • Since this drug contains lactose, genetic problems such as galactose intolerance, Lapp lactase deficiency, glucose-galactose malabsorption, etc
  • active liver disease

研究组 & 干预措施

experimental group

Experimental

naltrexone 50mg

干预措施: Naltrexone (Drug)

comparison group

Placebo Comparator

placebo

干预措施: Placebo (Drug)

结局指标

主要结局

Frequency of nonsuicidal self-injurous behavior

时间窗: 6 weeks

Total number of nonsuicidal self-injurous behavior during study period

次要结局

  • Clinical Global Impressions(6 weeks)
  • Obsessive Compulsive Drinking Scale(6 weeks)
  • Eating Disorder Examination-Questionnaire(6 weeks)
  • Deliberate Self-harm Inventory(6 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Yong Min Ahn

Professor

Seoul National University Hospital

研究点 (2)

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